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Research 121–150 of 844
- The Application of Light Emitting Diode (LED) in Cosmetic Dermatology
- Alopecia Areata: Understanding the Pathophysiology and Advancements in Treatment Modalities
- Diagnosis and treatment of cutaneous adverse effects of targeted therapy, antibody–drug conjugates, and immunotherapy in cancer patients: a national consensus statement by the Spanish Society of Medical Oncology and the Spanish Academy of Dermatology and Venereology
- Scarring Alopecia in a 66‐Year‐Old Woman
- Stem-cell therapy in dermatology – Challenges and opportunities
- Tyrosine kinase Inhibitors in Dermatology: A Systemic Review
- Profibrotic Subsets of SPP1+ Macrophages and POSTN+ Fibroblasts Contribute to Fibrotic Scarring in Acne Keloidalis
- Cannabinoid Signaling in the Skin: Therapeutic Potential of the “C(ut)annabinoid” System
- Stem Cell Therapies for Epidermolysis Bullosa Treatment
- A Heritable Keratinization Defect of the Superficial Epidermis in Norfolk Terriers
- Pili Torti: A Feature of Numerous Congenital and Acquired Conditions
- Cutaneous Side Effects of Modern Targeted Therapy and Immunotherapy in Patients with Dermatological Malignancies
- Treatment of pediatric alopecia areata: A systematic review
- Cicatricial (Scarring) Alopecias
- Hair and Nail Relationship
- Lasers in dermatology
- Weeping Wound, Disgruntled Gut and Fading Hunger: Acrodermatitis Enteropathica in an Infant
- LUPUS ERYTHEMATOSUS AND THE SKIN
- Two Dogs with Juvenile-Onset Skin Diseases with Involvement of Extremities
- Neuroendocrine Controls of Keratin Expression in Human Skin
- The Functional Diversity of Epidermal Keratins Revealed by the Partial Rescue of the Keratin 14 Null Phenotype by Keratin 16
- Deficient Plakophilin-1 Expression Due to a Mutation in PKP1 Causes Ectodermal Dysplasia-Skin Fragility Syndrome in Chesapeake Bay Retriever Dogs
- Harnessing neuroendocrine controls of keratin expression: A new therapeutic strategy for skin diseases?
- Analysis of the relationship between the mutation site of the SLC39A4 gene and acrodermatitis enteropathica by reporting a rare Chinese twin: a case report and review of the literature
- Oral Presentations
- SUMMARIES OF PAPERS
- 688 Precise and efficient editing of the COL7A1 gene in RDEB derived iPSCs with CRISPR/Cas9 and prime editing
- Pellagra and anorexia nervosa: a case report
- Ichthyosis with confetti: a rare diagnosis and treatment plan
- Localized Epidermolysis Bullosa Simplex (Weber-Cockayne type)